Literature DB >> 10206641

Exposing the human nude phenotype.

J Frank, C Pignata, A A Panteleyev, D M Prowse, H Baden, L Weiner, L Gaetaniello, W Ahmad, N Pozzi, P B Cserhalmi-Friedman, V M Aita, H Uyttendaele, D Gordon, J Ott, J L Brissette, A M Christiano.   

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Year:  1999        PMID： 10206641     DOI： 10.1038/18997

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  58 in total

1.  The nude mutant gene Foxn1 is a HOXC13 regulatory target during hair follicle and nail differentiation.

Authors:  Christopher S Potter; Nathanael D Pruett; Michael J Kern; Mary Ann Baybo; Alan R Godwin; Kathleen A Potter; Ron L Peterson; John P Sundberg; Alexander Awgulewitsch
Journal:  J Invest Dermatol       Date:  2010-12-30       Impact factor: 8.551

Review 2.  In control of biology: of mice, men and Foxes.

Authors:  Patrick J E C Wijchers; J Peter H Burbach; Marten P Smidt
Journal:  Biochem J       Date:  2006-07-15       Impact factor: 3.857

3.  First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases.

Authors:  M Louise Markert; José G Marques; Bénédicte Neven; Blythe H Devlin; Elizabeth A McCarthy; Ivan K Chinn; Adriana S Albuquerque; Susana L Silva; Claudio Pignata; Geneviève de Saint Basile; Rui M Victorino; Capucine Picard; Marianne Debre; Nizar Mahlaoui; Alain Fischer; Ana E Sousa
Journal:  Blood       Date:  2010-10-26       Impact factor: 22.113

Review 4.  [Genetically induced hair diseases].

Authors:  T Wiederholt; P Poblete-Gutiérrez; J Frank
Journal:  Hautarzt       Date:  2003-07-04       Impact factor: 0.751

5.  Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex.

Authors:  Maria-Teresa Romano; Aylar Tafazzoli; Maximilian Mattern; Sugirthan Sivalingam; Sabrina Wolf; Alexander Rupp; Holger Thiele; Janine Altmüller; Peter Nürnberg; Jürgen Ellwanger; Reto Gambon; Alessandra Baumer; Nicolai Kohlschmidt; Dieter Metze; Stefan Holdenrieder; Ralf Paus; Dieter Lütjohann; Jorge Frank; Matthias Geyer; Marta Bertolini; Pavlos Kokordelis; Regina C Betz
Journal:  Am J Hum Genet       Date:  2018-10-25       Impact factor: 11.025

6.  Postnatal tissue-specific disruption of transcription factor FoxN1 triggers acute thymic atrophy.

Authors:  Lili Cheng; Jianfei Guo; Liguang Sun; Jian Fu; Peter F Barnes; Daniel Metzger; Pierre Chambon; Robert G Oshima; Takashi Amagai; Dong-Ming Su
Journal:  J Biol Chem       Date:  2009-12-02       Impact factor: 5.157

Review 7.  [Genetic hair diseases. An update].

Authors:  J Frank; P Poblete-Gutiérrez; K Giehl
Journal:  Hautarzt       Date:  2013-11       Impact factor: 0.751

Review 8.  Using the ENCODE Resource for Functional Annotation of Genetic Variants.

Authors:  Michael J Pazin
Journal:  Cold Spring Harb Protoc       Date:  2015-03-11

9.  Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.

Authors:  Zhimiao Lin; Quan Chen; Lei Shi; Mingyang Lee; Kathrin A Giehl; Zhanli Tang; Huijun Wang; Jie Zhang; Jinghua Yin; Lingshen Wu; Ruo Xiao; Xuanzhu Liu; Lanlan Dai; Xuejun Zhu; Ruoyu Li; Regina C Betz; Xue Zhang; Yong Yang
Journal:  Am J Hum Genet       Date:  2012-10-11       Impact factor: 11.025

Review 10.  Genetics of SCID.

Authors:  Fausto Cossu
Journal:  Ital J Pediatr       Date:  2010-11-15       Impact factor: 2.638
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